ENST00000342992.11:c.96635C>A
(TTN)
|
ENSP00000343764.6:p.Thr32212Asn
|
|
ENST00000342175.11:c.77720C>A
(TTN)
|
ENSP00000340554.6:p.Thr25907Asn
|
|
ENST00000359218.10:c.77519C>A
(TTN)
|
ENSP00000352154.5:p.Thr25840Asn
|
|
ENST00000342175.10:c.77720C>A
(TTN)
|
ENSP00000340554.6:p.Thr25907Asn
|
|
ENST00000342992.10:c.96635C>A
(TTN)
|
ENSP00000343764.6:p.Thr32212Asn
|
|
ENST00000359218.9:c.77519C>A
(TTN)
|
ENSP00000352154.5:p.Thr25840Asn
|
|
ENST00000460472.6:c.77144C>A
(TTN)
|
ENSP00000434586.1:p.Thr25715Asn
|
|
ENST00000589042.5:c.104339C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr34780Asn
|
|
ENST00000591111.5:c.99416C>A
(TTN)
|
ENSP00000465570.1:p.Thr33139Asn
|
|
ENST00000615779.4:c.99416C>A
(TTN)
|
ENSP00000483597.1:p.Thr33139Asn
|
|
NM_001256850.1:c.99416C>A
(TTN)
|
NP_001243779.1:p.Thr33139Asn
|
|
NM_001267550.2:c.104339C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Thr34780Asn
|
|
NM_003319.4:c.77144C>A
(TTN)
|
NP_003310.4:p.Thr25715Asn
|
|
NM_133378.4:c.96635C>A
(TTN)
|
NP_596869.4:p.Thr32212Asn
|
|
NM_133432.3:c.77519C>A
(TTN)
|
NP_597676.3:p.Thr25840Asn
|
|
NM_133437.4:c.77720C>A
(TTN)
|
NP_597681.4:p.Thr25907Asn
|
|
NR_038271.1:n.446+8640G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3456G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.103436C>A
(TTN)
|
XP_011510031.1:p.Thr34479Asn
|
|
XM_011511730.1:c.77330C>A
(TTN)
|
XP_011510032.1:p.Thr25777Asn
|
|
XM_011511731.1:c.77189C>A
(TTN)
|
XP_011510033.1:p.Thr25730Asn
|
|
XM_017004819.1:c.103232C>A
(TTN)
|
XP_016860308.1:p.Thr34411Asn
|
|
XM_017004820.1:c.98630C>A
(TTN)
|
XP_016860309.1:p.Thr32877Asn
|
|
XM_017004821.1:c.98627C>A
(TTN)
|
XP_016860310.1:p.Thr32876Asn
|
|
XM_017004822.1:c.95669C>A
(TTN)
|
XP_016860311.1:p.Thr31890Asn
|
|
XM_017004823.1:c.77285C>A
(TTN)
|
XP_016860312.1:p.Thr25762Asn
|
|
XM_024453094.1:c.98780C>A
(TTN)
|
XP_024308862.1:p.Thr32927Asn
|
|
XM_024453095.1:c.98777C>A
(TTN)
|
XP_024308863.1:p.Thr32926Asn
|
|
XM_024453096.1:c.98210C>A
(TTN)
|
XP_024308864.1:p.Thr32737Asn
|
|
XM_024453097.1:c.95552C>A
(TTN)
|
XP_024308865.1:p.Thr31851Asn
|
|
XM_024453098.1:c.95471C>A
(TTN)
|
XP_024308866.1:p.Thr31824Asn
|
|
XM_024453099.1:c.77234C>A
(TTN)
|
XP_024308867.1:p.Thr25745Asn
|
|
XM_024453100.1:c.67088C>A
(TTN)
|
XP_024308868.1:p.Thr22363Asn
|
|